| Literature DB >> 29166549 |
Christian Marquardt1, Oliver Hegen1, Ariane Vogel1, Andreas Stauber1, Michael Bodensteiner1, Alexey Y Timoshkin2, Manfred Scheer1.
Abstract
We report on depolymerization reactions of poly(phosphinoboranes). The cleavage of the polymers [H2 PBH2 ]n (2 a), [tBuHPBH2 ]n (2 c), [PhHPBH2 ]n (2 e) and the oligomer [Ph2 PBH2 ]n (2 b), with strong Lewis bases (LBs), in particular with NHCs, leads to the corresponding monomeric phosphanylboranes R1 R2 PBH2 LB. It is observed that the depolymerization depends on the strength and stability of the LBs as well as on the substitution pattern of the poly(phosphinoboranes). The solid state structures of the monomeric phosphinoboranes H2 PBH2 NHCMe (NHC=N-heterocyclic carbene) (4 a), H2 PBH2 NHCdipp (5 a) and tBuHPBH2 NHCMe (4 c) were determined. DFT calculations support the experimentally observed reaction behavior.Entities:
Keywords: Lewis bases; boranes; carbenes; cleavage reactions; phosphorus
Year: 2017 PMID: 29166549 DOI: 10.1002/chem.201705510
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236